Development and clinical application of high performance liquid chromatography for the simultaneous determination of plasma levels of theophylline and its metabolites without interference from caffeine

A high performance liquid chromatography (HPLC) method has been developed for the simultaneous determination of plasma levels of theophylline and its metabolites without interference from caffeine or caffeine metabolites. The method is simple and of practical use because it is applicable even to plasma samples from patients who take caffeine-containing beverages. The method was also reproducible with a coefficient of variation of less than 5% for each analyte. The levels of theophylline, determined by HPLC, were validated by their high correlation to the levels obtained by fluorescence polarization immunoassay. HPLC was used to determine theophylline levels in patients with bronchial asthma. The data revealed that the ratio of 1,3-dimethyluric acid, the major metabolite of theophylline, to theophylline concentration in the plasma was within a narrow range in most patients (0.055 +/- 0.01, n = 66), regardless of the method of theophylline administration or the time of blood sampling. Conversely, this ratio was as low as 0.027 +/- 0.005 in the patient with a long plasma half-life of theophylline. These results suggest that it may be possible to predict the plasma half-life of theophylline for each patient from a single blood sample. This may be useful when planning theophylline administration, especially in patients with abnormal theophylline metabolism.     

New addresses on an addressable virus nanoblock; uniquely reactive Lys residues on cowpea mosaic virus

Cowpea mosaic virus (CPMV) is a robust, icosahedrally symmetric platform successfully used for attaching a variety of molecular substrates including proteins, fluorescent labels, and metals. The symmetric distribution and high local concentration of the attached molecules generates novel properties for the 30 nm particles. We report new CPMV reagent particles generated by systematic replacement of surface lysines with arginine residues. The relative reactivity of each lysine on the native particle was determined, and the two most reactive lysine residues were then created as single attachment sites by replacing all other lysines with arginine residues. Structural analysis of gold derivatization not only corroborated the specific reactivity of these unique lysine residues but also demonstrated their dramatically different presentation environment. Combined with site-directed cystine mutations, it is now possible to uniquely double label CPMV, expanding its use as an addressable nanoblock.     

Spatial profile measurement of ionization and excitation temperatures in an inductively coupled plasma

The developed instrument for spatial profile measurement [1] has been applied to the measurement of ionization and excitation temperatures in an inductively coupled plasma (ICP). The silicon intensified target (SIT) detector allowed it to measure a large number of emission spectra in a short period. The ease of acquisition enabled building up complete contour maps of ionization and excitation temperatures. The contour maps of various temperatures reveal that local thermal equilibrium does not exist in the whole ICP. The comparison between ionization temperature profiles for Ar and Ca indicates that in the normal analytical zone of the ICP, Ca is ionized as expected from the Ar ionization temperature. Excitation temperatures derived from low-level Fe I lines are lower than those derived from high-level Fe I lines over a large part of the plasma. The result confirms that for Fe I lines the ICP is characterized as an ionizing plasma in the whole ICP and the low atomic levels are overpopulated with respect to the high atomic levels.     

Tailor-made UV-curable powder clear coatings for metal applications

UV-curable powder coatings combine most of the benefits of conventional powder coatings together with the advantages of radiation-curable liquid coatings. This new coating process is not only environmentally friendly. It can also be used to coat substrates like wood, plastic, glass or metal at low temperatures within a short curing time. Several coatings based on binders like urethane vinylethers/unsaturated polyesters or methacrylates are developed for metals, wood or pvc flooring. This paper describes urethane acrylates as a new resin system for UV-curable powder clear coatings. The binders can be amorphous or (semi)crystalline. By combining both types it is possible to get tailor-made binders which exhibit an unique coating performance of excellent adhesion, good flexibility and high hardness on metal substrates. The appearance of the clear coatings can be varied from high to low translucent. In addition, the coatings show a good weatherability.     

Experimental investigation of beam heating in a soft X-ray scanning transmission X-ray microscope

A variable temperature sample holder with an operational range of 15 to 200 °C and an accuracy of ±1 °C has been fabricated for scanning transmission X-ray microscopes (STXM). Here we describe the device, and use it to image the polycrystalline morphology of solid stearic acid and palmitic acid at temperatures near their respective melting points as a means of checking for possible sample heating caused by the focused X-ray beam. The melting points observed in STXM were identical to those observed by conventional methods within measurement uncertainty, even under the most extreme, high dose rate imaging conditions investigated. The beam-induced temperature rise in the sample is inferred to be below 1 °C for dose rates of up to 2.7 GGy/s.     

High-temperature micro liquid chromatography for lipid molecular species analysis with evaporative light scattering detection

The need for a rapid and sensitive chromatographic technique for analyzing lipid molecular species, has led to the development of an high-temperature micro liquid chromatographic system (HTLC) coupled to an evaporative light scattering detector. The increased diffusion coefficients and reduced viscosity at higher temperatures allowed lipids to be analyzed rapidly with solvents differing from those classically used in lipids chemistry. Hypercarb, a reverse phase material, was used for its different properties including heat resistance in high temperature micro HPLC. We have investigated the temperature effect on kinetic performances in HTLC, established pure solvents eluent strength at high temperature and studied different classes of lipids with seven pure solvents. We found that it was possible to use alcohols solvents in the mobile phase to elute lipids without the use of chlorinated solvents. A quick and simple method was developed to analyze a complex lipid simple, ceramide type III and type IV.     

Pressurised fluid extraction (PFE) as an alternative general method for the determination of pesticide residues in rape seed

A pressurised fluid extraction (PFE) multi-method has been developed for the determination of pesticide residues in rape seed. The method was validated for 25 different pesticides and metabolites. The reliability and efficiency of PFE for extracting pesticide residues from rape seed was investigated. The traditional extraction solvent, hexane saturated with acetonitrile, was used at elevated temperature and pressure. With increased temperature, the extraction kinetics were improved but at the same time more co-extractives were obtained in the form of lipids. When 1 g of rape seed was extracted at temperatures from 60 degrees C to 150 degrees C, the lipid content extracted was found to be as high as 17-26%. An additional clean-up step was therefore required and lipid co-extractives were effectively removed by gel permeation chromatography. The interpretation of the chromatograms and the quantification of the results were satisfactorily improved by the removal of interfering lipids. The developed method was used to extract vinclozolin and iprodione from incurred samples, resulting in a concentration in accordance with the results using conventional liquid-liquid extraction (LLE) between hexane and acetonitrile and also supercritical fluid extraction (SFE) using carbon dioxide. The results of the present study suggest that PEE is a good alternative extraction technique for the determination of pesticide residues in oil seed. Despite the necessity for a lipid-removal clean-up step, the PFE technique facilitated the extraction process by faster extractions and the possibility of automated analysis.     

New polyimide ultrafiltration membranes for organic use

A solvent-resistant membrane for use in ultrafiltration processes has recently been developed by Nitro. The membrane is made from a new polyimide that can be synthesized from 1,2,3,4-butane tetracarboxylic acid and an aromatic diamine. This membrane exhibits excellent stability and high fluxes with most common organic solvents, even when tested at elevated temperatures.     

Development of septum-free injector for gas chromatography and its application to the samples with a high boiling point

A novel apparatus with a simple structure has been developed for introducing samples into the vaporizing chamber of a gas chromatograph. It requires no septum due to the gas sealing structure over the carrier gas supply line. The septum-free injector made it possible to use injection port temperatures as high as 450 degrees C. Repetitive injection of samples with boiling points below 300 degrees C resulted in peak areas with relative standard deviations between 1.25 and 3.28% (n=5) and good linearity (r(2)>0.9942) for the calibration curve. In the analysis of polycyclic aromatic hydrocarbons and a base oil, the peak areas of components with high boiling points increased as the injection port temperature was increased to 450 degrees C.     

Aerobic Oxidative N-Heterocyclic Carbene Catalysis

The ease with which simple starting materials can be transformed into highly functionalized products has made oxidative N-heterocyclic carbene (NHC) catalysis an area of significant interest. However, the use of stoichiometric amounts of high molecular weight oxidants in most reactions generates an undesired equivalent amount of waste. To address this issue, the use of oxygen as the terminal oxidant in NHC catalysis has been developed. Oxygen is attractive due to its low cost, low molecular weight, and ability to generate water as the sole by-product. However, molecular oxygen is challenging to use as a reagent in organic synthesis due to its unreactive ground state, which often requires reactions to be run at high temperatures and results in the formation of kinetic side-products. This review covers the development of aerobic oxidative carbene catalysis, including NHC-catalyzed reactions with oxygen, strategies for oxygen activation, and selectivity issues under aerobic conditions.     

Confined high-pressure chemical deposition of hydrogenated amorphous silicon

Hydrogenated amorphous silicon (a-Si:H) is one of the most technologically important semiconductors. The challenge in producing it from SiH(4) precursor is to overcome a significant kinetic barrier to decomposition at a low enough temperature to allow for hydrogen incorporation into a deposited film. The use of high precursor concentrations is one possible means to increase reaction rates at low enough temperatures, but in conventional reactors such an approach produces large numbers of homogeneously nucleated particles in the gas phase, rather than the desired heterogeneous deposition on a surface. We report that deposition in confined micro-/nanoreactors overcomes this difficulty, allowing for the use of silane concentrations many orders of magnitude higher than conventionally employed while still realizing well-developed films. a-Si:H micro-/nanowires can be deposited in this way in extreme aspect ratio, small-diameter optical fiber capillary templates. The semiconductor materials deposited have ~0.5 atom% hydrogen with passivated dangling bonds and good electronic properties. They should be suitable for a wide range of photonic and electronic applications such as nonlinear optical fibers and solar cells.     

Development of an on-line isotope dilution technique with HPLC/ICP-MS for the accurate determination of elemental species

An on-line isotope dilution technique has been developed for use with a high performance liquid chromatography system (HPLC) coupled to an inductively coupled plasma mass spectrometer (ICP-MS). With this method it is possible to characterize elemental species at low concentration levels and to quantify them accurately. The possibilities of this method are shown using the examples of the determination of the interactions of different molecular weight fractions of dissolved organic matter (DOM) with copper and molybdenum in a natural water sample.     

Determination of glass-transition temperatures of polymers: A modified computational scheme

A modified computational scheme is developed for estimation of the glass-transition temperatures of linear and network polymers. Contributions of atoms and atomic groups involved in the main chain and side chains of a polymer are separated. The suggested scheme makes it possible to avoid multiple corrections immanent to earlier advanced glass-transition temperature calculation models. The calculated and experimental values of glass-transition temperatures for polymers of the most diverse classes are in a good agreement; R ² is 0.998. This scheme makes it possible to substantially simplify calculations, and it is applicable to polymers of all chemical structures with repeating units containing elements C, H, O, N, F, Cl, Si, and S.     

Electrochemical sensor for the detection and presumptive identification of quinolone and tetracycline residues in milk

A novel application of an electrochemical biosensor is here employed as analytical method for the detection and presumptive identification of antimicrobial drug residues in milk. The measurement was based on carbon dioxide production rate in relation to inhibition of microbial grow (Escherichia coli ATCC 11303). In this pilot study quinolone and tetracycline residues have been taken into consideration because use of these last in livestock production has been identified as area of particular concern. The experimental approach and analytical method developed appear adequate for the purpose, and compared to older screening methods as, for example, the microbial inhibition assays and immunoassays, offers the advantages of (i) very short analysis time (about 120 min); (ii) smaller sample amount (approximately 0.5 mL); (iii) no sample treatment (iv) good precision; and (v) the possibility of following, in a continuous manner, the inhibition process. Moreover, sensitivity of electrochemical biosensor system is resulted very high considering that for all quinolones and tetracyclines investigated it has been possible detect a residue concentration below or equal to 25 μg L⁻¹. Under this point of view, it must be considered that the maximum residue limits fixed by UE for quinolones and tetracyclines in milk are, at present, all higher of this concentration.     

The use of FT-IR as a screening technique for organic residue analysis of archaeological samples

A range of archaeological samples have been examined using FT-IR spectroscopy. These include suspected coprolite samples from the Neolithic site of Catalh?yük in Turkey, pottery samples from the Roman site of Silchester, UK and the Bronze Age site of Gatas, Spain and unidentified black residues on pottery sherds from the Roman sites of Springhead and Cambourne, UK. For coprolite samples the aim of FT-IR analysis is identification. Identification of coprolites in the field is based on their distinct orange colour; however, such visual identifications can often be misleading due to their similarity with deposits such as ochre and clay. For pottery the aim is to screen those samples that might contain high levels of organic residues which would be suitable for GC-MS analysis. The experiments have shown coprolites to have distinctive spectra, containing strong peaks from calcite, phosphate and quartz; the presence of phosphorus may be confirmed by SEM-EDX analysis. Pottery containing organic residues of plant and animal origin has also been shown to generally display strong phosphate peaks. FT-IR has distinguished between organic resin and non-organic compositions for the black residues, with differences also being seen between organic samples that have the same physical appearance. Further analysis by GC-MS has confirmed the identification of the coprolites through the presence of coprostanol and bile acids, and shows that the majority of organic pottery residues are either fatty acids or mono- or di-acylglycerols from foodstuffs, or triterpenoid resin compounds exposed to high temperatures. One suspected resin sample was shown to contain no organic residues, and it is seen that resin samples with similar physical appearances have different chemical compositions. FT-IR is proposed as a quick and cheap method of screening archaeological samples before subjecting them to the more expensive and time-consuming method of GC-MS. This will eliminate inorganic samples such as clays and ochre from GC-MS analysis, and will screen those samples which are most likely to have a high concentration of preserved organic residues.     

Determination of fourteen non-steroidal anti-inflammatory drugs in animal serum and plasma by liquid chromatography/mass spectrometry

The European Union has regulated the use of non-steroidal anti-inflammatory drugs (NSAIDs) in animal production and requires its member states to detect their residues in different matrices. In this work, a detailed MS and MS/MS study by ion-trap mass spectrometry of fourteen NSAIDs is described. Two multi-residue reversed-phase LC/ESI-MS/MS methods were developed, one for the determination of salicylic acid, naproxen, carprofen, flurbiprofen, ibuprofen, niflumic acid and meclofenamic acid in the negative ion mode, and the other for the determination of ketoprofen, suxibutazone, diclofenac, mefenamic acid, tolfenamic acid, phenylbutazone and its metabolite oxyphenbutazone in the positive ion mode. It was thus possible to confirm up to 14 different NSAID residues in serum and plasma samples of farmed animals, after chromatographic separation by a linear gradient. These substances were chosen as representative of different chemical subclasses of NSAIDs. The two methods were also validated in-house at three contamination levels, evaluating specificity and calculating mean recoveries, repeatability and within-laboratory reproducibility. The MS/MS product ion spectra were successfully used for the qualitative identification of all the drugs tested. All the NSAIDs, apart from salicylic acid, were recovered in high amounts, ranging between 71.6% and 100.9%.     

The Effect of Temperature on the Plasma-Catalytic Destruction of Propane and Propene: A Comparison with Thermal Catalysis

A comparison has been made of plasma-catalysis with thermal-catalysis and plasma alone for the removal of low concentrations of propane and propene from synthetic air using a one-stage, catalyst-in discharge configuration. In all cases, plasma-catalysis produces better hydrocarbon destructions (~40%) than thermal catalysis at low temperatures. At higher temperatures, little difference is observed between plasma-catalytic and thermal-catalytic operation. Plasma operation by itself had a similar effectiveness to plasma-catalysis at low temperatures but was significantly lower (up to 50%) as the temperature was raised. By examining the form of the temperature dependence for the plasma-catalytic destruction processes, it is possible to phenomenologically distinguish two contributions to the destruction; one that is specifically plasma-induced and another (at higher temperatures) in which both plasma and thermal activation have similar mechanisms.     

Non-thermal plasma technology for the conversion of CO2

The conversion of carbon dioxide is vital if we are to avoid the catastrophic consequences that will result from further global temperature rise as a result of burning fossil fuels. Current techniques, such as catalytic conversion and biochemical processes, are each associated with their own drawbacks such as catalyst deactivation and high energy input. Plasma processes are gaining increasing interest as they have the potential to reduce a greater amount of atmospheric environmental pollutants at any one time due to an increased throughput, whilst using a smaller reactor with improved energy efficiency and near-zero emissions. Non-thermal plasma can dissociate stable molecules, such as CO₂, at temperatures as low as room temperature. It is this key feature which makes plasma conversion such a promising technology in the conversion and utilisation of CO₂. Furthermore, possible products from plasma processes include fuels and chemicals, such as methanol and syngas, which have a high market value; hence potentially making the process feasible on an industrial scale. This paper discusses recent advances in the use of plasma processes for carbon dioxide conversion, along with the future outlook of this technology and the impact these techniques could have on the chemical and energy industries.